Ca(2+)-activated anion channels and membrane depolarizations induced by blue light and cold in Arabidopsis seedlings

Plant Physiol. 1997 Aug;114(4):1327-34. doi: 10.1104/pp.114.4.1327.

Abstract

The activation of an anion channel in the plasma membrane of Arabidopsis thaliana hypocotyls by blue light (BL) is believed to be a signal-transducing event leading to growth inhibition. Here we report that the open probability of this particular anion channel depends on cytoplasmic Ca2+ ([Ca2+]cyt) within the concentration range of 1 to 10 microM, raising the possibility that BL activates the anion channel by increasing [Ca2+]cyt. Arabidopsis seedlings cytoplasmically expressing aequorin were generated to test this possibility. Aequorin luminescence did not increase during or after BL, providing evidence that Ca2+ does not play a second-messenger role in the activation of anion channels. However, cold shock simultaneously triggered a large increase in [Ca2+]cyt and a 110-mV transient depolarization of the plasma membrane. A blocker of the anion channel, 5-nitro-2-(3-phenylpropylamino)-benzoic acid, blocked 61% of the cold-induced depolarization without affecting the increase in [Ca2+]cyt. These data led us to propose that cold shock opens Ca2+ channels at the plasma membrane, allowing an inward, depolarizing Ca2+ current. The resulting large increase in [Ca2+]cyt activates the anion channel, which further depolarizes the membrane. Although an increase in [Ca2+]cyt may activate anion channels in response to cold, it appears that BL does so via a Ca(2+)-independent pathway.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aequorin / genetics
  • Aequorin / metabolism
  • Anions
  • Arabidopsis / metabolism
  • Calcium / metabolism*
  • Cold Temperature*
  • Ion Channels / antagonists & inhibitors
  • Ion Channels / metabolism
  • Ion Channels / radiation effects*
  • Light*
  • Membrane Potentials / radiation effects*
  • Nitrobenzoates / pharmacology
  • Plants, Genetically Modified
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • Anions
  • Ion Channels
  • Nitrobenzoates
  • Recombinant Proteins
  • 5-nitro-2-(3-phenylpropylamino)benzoic acid
  • Aequorin
  • Calcium